| ¿µ¹® | nevus | ÇÑ±Û | ¸ð¹Ý |
|---|---|---|---|
| ¼³¸í | ¼±Ãµ¼ºÀ¸·Î ³ªÅ¸³ª´Â ÇǺÎÀÇ Á¡. À̸¥¹Ù ¸ð¹Ý¼¼Æ÷(nevus cell: ¸á¶ó´Ñ ¼¼Æ÷¿Í ºñ½ÁÇÏÁö¸¸ Á¶±Ý ´Ù¸¥, °°Àº °èÅëÀÇ º¯Çü¼¼Æ÷)¿¡ ÀÇÇØ ³ªÅ¸³ª¸ç, ÀϺο¡¼´Â ¾Ç¼ºÈæ»öÁ¾(malignant melanoma)À¸·Î º¯ÈÇÒ ¼öµµ ÀÖ´Ù. Ä¡·á´Â ¿Ü°úÀû ÀýÁ¦ÀÌ´Ù. |
||
| DMN | dimethylnitrosamine; dorsal motor nucleus; dysplastic melanocytic nevus |
|---|---|
| DNS | deviated nasal septum; diaphragmatic nerve stimulation; did not show [for appointment]; Doctor of Nu... |
| IMDS | Idiopathic Myelo-Dysplastic Syndrome = Preleukemia = Refractory Anemi... |
| MDS | Myelo-Dysplastic Syndrome = Refractory (Dysmyelopoietic) Anemia = (Id... |
| MCDK | multicystic dysplastic kidney |
| BCNS | Basal Cell Nevus Syndrome |
|---|---|
| BRBNS | Blue Rubber Bleb Nevus Syndrome |
| DNS | Dysplastic Naevus Syndrome |
| DMN | Dysplastic melanocytic nevi |
| DN | Dysplastic naevi |
| dysplastic nevus | <syndrome> Clinically atypical nevi (usually exceeding 5 mm in diameter and having variable pigmentation and ill defined borders) with an increased risk for development of non-familial cutaneous malignant melanoma. Biopsies show melanocytic dysplasia. Nevi are clinically and histologically identical to the precursor lesions for melanoma in the b-k mole syndrome. (12 Dec 1998) |
|---|---|
| dysplastic nevus syndrome | <syndrome> Clinically atypical nevi (usually exceeding 5 mm in diameter and having variable pigmentation and ill defined borders) with an increased risk for development of non-familial cutaneous malignant melanoma. Biopsies show melanocytic dysplasia. Nevi are clinically and histologically identical to the precursor lesions for melanoma in the b-k mole syndrome. (12 Dec 1998) |
| multicystic dysplastic kidney disease | <radiology> most severe form of renal dysplasia, most common cause of palpaple abdominal mass in infants, unilateral (almost always; if bilateral, death occurs in utero), ureter absent or atretic, not associated with other cysts or with periportal fibrosis, Potter type II (12 Dec 1998) |
|---|---|
| congenital dysplastic angiectasia | <syndrome> A congenital malformation syndrome characterised by the triad of asymmetric limb hypertrophy, haemangiomata, and nevi. Asymmetric limb hypertrophy is enlargement of one limb and not the corresponding limb on the other side, the enlarged limb being 3 times more likely to be a leg than an arm in ktw; and the limb enlargement is of bone as well as soft tissue. The haemangiomas, abnormal nests of blood vessels that proliferate inappropriately and excessively, cover a remarkable range from small innocuous capillary haemangiomas ( strawberry marks ) to huge cavernous haemangiomas. The nevi are pigmented moles on the skin; in ktw there are often also dark linear streaks on the skin, streaks due to too much pigment. There can be other abnormalities but the triad is the consistent clinical centrepiece of the disease. most persons with ktw have an enlarged leg and do relatively well without treatment or, for example, with only compression from an elastic stocking. Skin ulcers and other skin problems can occur over the swollen leg. Usually, the treatment is conservative. Surgery is almost never needed. The only possible exceptions are the very rare situations in which the leg reaches gigantic proportions or secondary clotting difficulties arise (due to trapping and destruction of blood platelets in a huge haemangioma). Then, amputation may become necessary. The cause of ktw syndrome is unknown. (12 Dec 1998) |
| congenital dysplastic angiomatosis | Autosomal dominant angiomatosis in which there is dysplasia of the underlying tissues, sometimes with overgrowth of bone (Klippel-Trenaunay-Weber syndrome), or encephalotrigeminal angiomatosis (Sturge-Weber syndrome) in which there is an angioma in the distribution of one or more branches of the trigeminal nerve, with vascular anomalies and calcification of the cerebral cortex. (05 Mar 2000) |
| dysplastic | Pertaining to or marked by dysplasia. (05 Mar 2000) |
| dysplastic nevi | Atypical moles; moles whose appearance is different from that of common moles. Dysplastic nevi are generally larger than ordinary moles and have irregular borders. Their colour often is not uniform; they usually are flat, but parts may be raised above the skin surface. (12 Dec 1998) |
| acquired nevus | A melanocytic nevus that is not visible at birth, but appears in childhood or adult life. (05 Mar 2000) |
| balloon cell nevus | A nevus in which many of the cells are large, with clear cytoplasm. (05 Mar 2000) |
| basal cell nevus | A hereditary disease noted in infancy or adolescence, characterised by lesions of the eyelids, nose, cheeks, neck, and axillae, appearing as uneroded flesh-coloured papules, some becoming pedunculated, and histologically indistinguishable from basal cell epithelioma; also noted are punctate keratotic lesions of the palms and soles; the lesions usually remain benign, but in some cases ulceration and invasion occur and are evidence of malignant change; autosomal dominant inheritance. (05 Mar 2000) |
| basal cell nevus syndrome | <syndrome> An inherited group of defects which involve abnormalities of the skin, eyes, nervous system, endocrine, glands and bones. The condition is characterised by an unusual facial appearance and a predisposition for skin cancer. (27 Sep 1997) |
| bathing trunk nevus | These large pigmented (often hairy) congenital nevi are important because of their increased risk (10 to 15%) of conversion into malignant melanoma. A biopsy can confirm if cells have turned malignant. Any change in a pre-existing nevus should prompt a physician evaluation. (27 Sep 1997) |
| Becker's nevus | A nevus first seen as an irregular pigmentation of the shoulders, upper chest, or scapular area, gradually enlarging irregularly and becoming thickened and hairy. Synonym: pigmented hair epidermal nevus. (05 Mar 2000) |
| blue nevus | A dark blue or blue-black nevus covered by smooth skin and formed by heavily pigmented spindle-shaped or dendritic melanocytes in the reticular dermis. Synonym: Jadassohn-Tieche nevus. (05 Mar 2000) |
| blue rubber bleb nevus syndrome | <radiology> Bean syndrome, sporadic (some autosomal dominant), rubbery, raised blue-black skin nevi (cavernous haemangiomata, 0.1 - 5 cm), GI mucosal haemangiomata, bowel: polypoid filling defects of varying sizes, visceral haemangiomata (by angio) associated with: leukaemia, medulloblastoma, hypernephroma, Mafucci syndrome More info: blue rubber bleb nevus syndrome (12 Dec 1998) |
| capillary nevus | Capillary haemangioma of the skin. (05 Mar 2000) |
| verrucous nevus | A skin-coloured or darker wartlike, often linear, lesion appearing at birth or early in childhood, and occurring in various sizes and locations, single or multiple. (05 Mar 2000) |
Synonyms : Dysplastic Nevi, B K Mole Syndrome, Dysplastic Nevus, Familial Atypical Multiple Mole Melanoma, Nevi, Dysplastic, Syndrome, B-K Mole, Syndrome, Dysplastic Nevus
| dysplastic nevus |
A mole with an unusual appearance; different from common moles
Ãâó: www.ehealthmd.com/library/melanoma/MEL_glossary.ht...
|
|---|---|
| dysplastic nevus |
an atypical mole that may be a precursor of malignant melanoma
Ãâó: www.beautysurg.com/resources/glossary_d.html
|
| dysplastic nevus syndrome |
A condition characterized by the presence of 100 or more moles on the upper trunk and limbs, at least one of which is dysplastic. The syndrome may be acquired or inherited. Individuals with DNS are at significantly increased risk of developing melanoma.
Ãâó: www.melanomacenter.org/glossary/d.html
|
| dysplastic nevus s. |
the occurrence of dysplastic nevi in persons with or at risk for familial or nonfamilial malignant melanoma.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|